SP Associates, Professional Employment Services

 

Specializing in Pharmaceuticals, Biotech, Medical Devices

 

Our Expertise Is In...

Home

Textiles:  Fibers, Non-Wovens, Composites

Pharmaceuticals and Biotech

Packaging, Pressure Sensitive

Medical Devices and Engineering

Contact Us

 

 

 

 

 

 

 

 

 

 

 

 

 

Back to the top

 

 

 

 

 

 

 

 

 

 

 

 

 

 

   

 

 

 

Back to the top

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

JOBS! | Send Us Your Resume | Email Me
Companies:  Let Us Know Your Key Personnel Needs

James Walkup, Executive Recruiter

Jim Walkup, Vice President, Executive Recruiter, BSBA from University of Alabama. Jim serves the Pharmaceutical, Medical Device, Biotech and Health and Beauty Aids Industries.

Jim recruits professional candidates, management, R&D Technical, QC/QA, manufacturing, engineering and other professionals for the above industries.

JOBS

Your resume is held in strict confidence, all fees are employer paid, and relocation assistance is provided for all qualified persons unless otherwise stated.

Updated February 2010

QC  HPLC Supervisor – 4 year science degree, prior management experience in GMP lab.  5 years experience utilizing HPLC in lab.  Supervise day-to-day activities of HPLC analytical staff.  Solid technical skills.   Responsible for all group functions: scheduling, testing, calibrations, instrument maintenance, inventory control, training, methods development, validations and participated hiring.  Conducts research, quantitative and qualitative analysis and experimentation.  Pennsylvania.  $50-60K
Business Development Manager-Sales – Company expanding contract bottling business of prescription, OTC and VMS products.  B.S.  5+ years experience developing contract packaging of pharmaceutical OTC and VMS sales and distribution of products.  Ability to develop new clients, both packaging (bottling) and distribution (3PL) of product.  Experience in soliciting and closing new business and highly developed interpersonal and business negotiation skills-proven track record.  Set and meet quarterly and annual sales budgets.  Charlotte, NC area.  Base salary depends on experience and knowledge, plus commission.
Sr. Process Engineer – Manager level.  Biological Sterile Validation Department.  Process validation activities and principles for sterile and vaccine manufacturing.  Validation oversight of new product introductions and new facility projects.  Will serve as subject matter expert for Process Validation which includes the development of strategies, standards, requirements, tools and templates.  BS, MS or PhD in Chemical Engineering, biochemistry or comparable.  Minimum 3 years direct responsibility for process validation of biologics and minimum 5 years experience with biological manufacturing processes.  Pennsylvania.  $90-125K.
R&D Quality Engineer – BS degree in Science or Engineering and 5 years in Pharma industry in quality Assurance, Regulatory Affairs, or Quality R&D.  this job functions in the new products division of the nutraceutical products group of this growing company.  Will be responsible for ensuring documented compliance of all applicable regulatory standards via generation, review and/or disposition of all innovation quality documentation.  Support new product development activities.  Design reviews and pre-validation assessment.  Charlotte, NC.  $70-75K base range, 8% bonus, plus relocation.
Quality Assurance Compliance Manager – BA/BS.  6-10 years experience with cGMP and regulated pharma industry practices: at least 6 years QA/Compliance, or AA with 8-10 years of A/Compliance experience.  Responsible for ensuring compliance to GMP principles, leading and participating in investigations, review/approval of process validation documents, and review/approval of equipment and software qualification/validation documents to ensure compliance with cGMPs, company procedures and regulatory commitments.  Florida.  $85-90K with bonus potential.  Relocation will be provided with sign-on bonus.  Temporary living assistance available.
Quality Assurance Manager – BS/MS in life sciences and related experience.  Supervise and support all signed personnel.  Assure that the technical departments are properly staffed to complete required tasks.  Evaluate capital expenditures necessary to maintain or improve departmental operations.  Interface with FDA investigators and other government officials during plant audits.  Maintain relations with customers to aid in compliance with regulators, or in development of new products.  Assist during customer audits of facility.  ANDA, FDA, DEA.  Florida.  $50-60K.
CMS Project Management – BS with at least 5 years working experience as project manager in GMP environment, pharma industry.  PMP Certification desired.  Oversee all project management activities within the Chemistry and Manufacturing Services department.  These include the development and optimization of project management systems within CMS to ensure communication and transparency throughout the organization.  The scope of the CMS project team includes the transfer of technology form the Product Development group, pharma process engineering, process scale-up, provides validation, building of launch quantities and post-approval changes.  Develop and optimize project management systems to meet diverse needs of CMS.  Manages project teams toward implementation of the operational plan.  PA.  $115K + bonus + relo package.
QA/QC/Regulatory Affairs-Pharma – BS Chemistry.  2 years experience in cGMP FDA regulated manufacturer.  Responsible for providing quality support to manufacturing, testing and releasing of products.  Auditing, cGMP.  Georgia.  $70-80K.
Formulator Scientist – BS/MS pharma.  Must have: 5-7 years formulation experience in a pharma science or food technology and 2-4 years experience with flavoring animal products or veterinary pharma.  Participate in multidisciplinary products development teams to advance early-stage development compounds.  Develop, design, balance flavor balance of veterinary application products.  SC.  $50-85K – full relocation.
QC Supervisor – BS Technical.  2-5 years experience packaging of contract pharma, OTC, VMS products.  Must have QC packaging experience.  Responsible for interviewing, hiring, training, coaching personnel.  Assure personnel follow safety rules, GMPs.  North Carolina.  $50K+ depending on experience.

Updated February 2010

SEND US YOUR RESUME

  • MS Word 95 or higher

  • Plain Text Format

Send Us Your Resume Now!

 

 

Toll Free:  (866)488-6677 | Phone:  (704)643-7250 | Fax:  (704)643-1249 | Email:  jwalkup@spassociates.com

Return to SP Associates | Textiles:  Fibers, Non-Wovens, Composites | Pharmaceuticals and Biotech | Packaging, Pressure Sensitive | Medical Devices and Engineering | Contact Us